Expression of tenascin, type IV collagen and laminin during human intrahepatic bile duct development and in intrahepatic cholangiocarcinoma

Expression of tenascin, type IV collagen and laminin during human intrahepatic bile duct development and in cholangiocarcinoma was examined by immunohistochemistry. In the developing hilar bile ducts, tenascin was expressed in the mesenchyme around the epithelial cells migrating from the ductal plate into the mesenchyme at 10–14 weeks of gestation. Tenascin was also expressed in the mesenchyme around newly formed hilar bile ducts at 15‐20 weeks of gestation, but its expression disappeared after 21 weeks of gestation. Type IV collagen and laminin were expressed around the ductal plate, around epithelial cells migrating from the ductal plate into the mesenchyme, and around newly formed hilar bile ducts, and their expression was present throughout fetal life. By contrast, in the development of peripheral bile ducts, tenascin expression was not found. Type IV collagen and laminin were identified around the ductal plate, migrating epithelial cells and peripheral bile ducts. In cholangiocarcinoma, tenascin and type IV collagen were expressed in the stroma, but laminin was not identified. These findings suggest that tenascin may play a role in hilar bile duct development and that type IV collagen and laminin may play a role in both hilar and peripheral bile duct development. Expression of tenascin and type IV collagen in the stroma of cholangiocarcinoma may be the result of malignant transformation of intrahepatic biliary epithelium; tenascin in peritumoral stroma may stimulate carcinoma cell proliferation and growth in cholangiocarcinoma.

[1]  P. Amenta,et al.  The extracellular matrix in hepatic regeneration. Localization of collagen types I, III, IV, laminin, and fibronectin. , 1991, Laboratory investigation; a journal of technical methods and pathology.

[2]  M. Chiquet,et al.  Chick myotendinous antigen. I. A monoclonal antibody as a marker for tendon and muscle morphogenesis , 1984, The Journal of cell biology.

[3]  M. Schwartz,et al.  Differential distribution of tenascin and cellular fibronectins in acute and chronic renal allograft rejection. , 1992, Laboratory investigation; a journal of technical methods and pathology.

[4]  R. Chiquet‐Ehrismann What distinguishes tenascin from fibronectin? , 1990, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[5]  Shigeki,et al.  Tenascin: cDNA cloning and induction by TGF‐beta. , 1988, The EMBO journal.

[6]  H. Popper,et al.  PROLIFERATION OF BILE DUCTS IN CIRRHOSIS. , 1964, Archives of pathology.

[7]  G M Edelman,et al.  A cDNA clone for cytotactin contains sequences similar to epidermal growth factor-like repeats and segments of fibronectin and fibrinogen. , 1988, Proceedings of the National Academy of Sciences of the United States of America.

[8]  J. Foidart,et al.  Distribution of extracellular matrix glycoproteins during normal development of human kidney. An immunohistochemical study. , 1986, Laboratory investigation; a journal of technical methods and pathology.

[9]  D. Schuppan,et al.  Structure of the Extracellular Matrix in Normal and Fibrotic Liver: Collagens and Glycoproteins , 1990, Seminars in liver disease.

[10]  M. Gerber,et al.  Development of intrahepatic bile ducts in humans. Possible role of laminin. , 1990, Archives of pathology & laboratory medicine.

[11]  V. Desmet Congenital diseases of intrahepatic bile ducts: Variations on the theme “ductal plate malformation” , 1992, Hepatology.

[12]  P. van Eyken,et al.  The development of the intrahepatic bile ducts in man: A keratin‐immunohistochemical study , 1988, Hepatology.

[13]  M. Basson,et al.  Extracellular matrix-cell interactions: dynamic modulators of cell, tissue and organism structure and function. , 1992, Laboratory investigation; a journal of technical methods and pathology.

[14]  T. Terada,et al.  Cystic dilatation of peribiliary glands in livers with adult polycystic disease and livers with solitary nonparasitic cysts: An autopsy study , 1992, Hepatology.

[15]  W. Halfter,et al.  Induction of tenascin in healing wounds , 1988, The Journal of cell biology.

[16]  R. Chiquet‐Ehrismann,et al.  Tenascin: an extracellular matrix protein involved in tissue interactions during fetal development and oncogenesis , 1986, Cell.

[17]  S. Tseng,et al.  Correlation of specific keratins with different types of epithelial differentiation: Monoclonal antibody studies , 1982, Cell.

[18]  E. Wisse,et al.  Localization and cellular source of the extracellular matrix protein tenascin in normal and fibrotic rat liver , 1992, Hepatology.

[19]  D. Schuppan,et al.  Light microscopic and ultrastructural distribution of type VI collagen in human liver: alterations in chronic biliary disease , 1992, Histopathology.

[20]  M. Gerber,et al.  Development of intrahepatic bile ducts in humans. Immunohistochemical study using monoclonal cytokeratin antibodies. , 1989, Archives of pathology & laboratory medicine.

[21]  M. Rojkind,et al.  Immunocytochemical localization of type B collagen: a component of basement membrane in human liver. , 1980, The American journal of pathology.

[22]  Shah Kd,et al.  Development of intrahepatic bile ducts in humans. Possible role of laminin. , 1990 .

[23]  P. van Eyken,et al.  Intrahepatic bile duct development in the rat: a cytokeratin-immunohistochemical study. , 1988, Laboratory investigation; a journal of technical methods and pathology.

[24]  T. Terada,et al.  Pathologic observations of intrahepatic peribiliary glands in 1,000 consecutive autopsy livers: IV. Hyperplasia of intramural and extramural glands. , 1992, Human pathology.

[25]  M. Bernfield,et al.  Basal lamina of embryonic salivary epithelia. Production by the epithelium and role in maintaining lobular morphology , 1977, The Journal of cell biology.

[26]  P. van Eyken,et al.  Expression of the novel extracellular matrix component tenascin in normal and diseased human liver. An immunohistochemical study. , 1990, Journal of hepatology.

[27]  J. Lemire,et al.  Cell lineages and oval cell progenitors in rat liver development. , 1991, Cancer research.

[28]  J. Engel EGF‐like domains in extracellular matrix proteins: Localized signals for growth and differentiation? , 1989, FEBS letters.

[29]  I. Virtanen,et al.  Differential distribution of tenascin in the normal, hyperplastic, and neoplastic breast. , 1990, Laboratory investigation; a journal of technical methods and pathology.

[30]  P. Ekblom,et al.  Tenascin during gut development: appearance in the mesenchyme, shift in molecular forms, and dependence on epithelial-mesenchymal interactions [published erratum appears in J Cell Biol 1989 Mar;108(3):following 1175] , 1988, The Journal of cell biology.

[31]  R. Timpl,et al.  Distribution of basement membrane proteins in normal and fibrotic human liver: collagen type IV, laminin, and fibronectin. , 1980, Gut.

[32]  T. Terada,et al.  Development of human intrahepatic peribiliary glands. Histological, keratin immunohistochemical, and mucus histochemical analyses. , 1993, Laboratory investigation; a journal of technical methods and pathology.

[33]  M. Kusakabe,et al.  Human Carcinoma Cells Synthesize and Secrete Tenascin in vitro , 1992, Japanese journal of cancer research : Gann.

[34]  P. Humphrey,et al.  Tenascin expression in prostatic hyperplasia, intraepithelial neoplasia, and carcinoma. , 1993, Human pathology.

[35]  I. Sugawara,et al.  Reduced tenascin expression in colonic carcinoma with lymphogenous metastasis. , 1991, Invasion & metastasis.

[36]  Antonio Martinez‐Hern Andez,et al.  The extracellular matrix in hepatic regeneration , 1995, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[37]  B. Gusterson,et al.  The distribution of immuno-reactive tenascin in the epithelial-mesenchymal junctional areas of benign and malignant squamous epithelia , 1990, Virchows Archiv. B, Cell pathology including molecular pathology.